Niemann-Pick disease: report of two cases and review of literature

被引：0

作者：

He, Wei ^{[1
]}

Wang, Zaoyu ^{[1
]}

Zhao, Ling ^{[1
]}

Xia, Jun ^{[1
]}

Liu, Qiang ^{[1
]}

机构：

[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Pathol, Shanghai 200127, Peoples R China

来源：

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2016年 / 9卷 / 01期

关键词：

Niemann-Pick Disease; hepatosplenomegaly; histochemical staining; vacuolation; C DISEASE; CLINICAL DESCRIPTION; IDENTIFICATION; BIOMARKERS;

D O I：

暂无

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Niemann-Pick Disease (NPD) refers to a group of disorders with deficiency in lipid storage, causing accumulation of fats in brain and liver that lead to serious damage or dysfunction of mentioned tissues. Its pathogenesis is still unclear, very rarely it has been associated with genetic disorders. Herein we report two cases: one is a 5-year-old boy and another is a 23-year-old woman.

引用

页码：296 / 301

页数：6

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